Vitrea Software Toshiba Package; VSTP-001A
K-Number: K171222 · 2017-06-08
ApplicantToshibamedical Systems Corporation
Decision Date2017-06-08
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Vitrea Software Toshiba Package; VSTP-001A is a medical device manufactured by Toshibamedical Systems Corporation. It received FDA 510(k) clearance on 2017-06-08 under approval number K171222. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Vitrea Software Toshiba Package; VSTP-001A?
Vitrea Software Toshiba Package; VSTP-001A is a medical device that received FDA 510(k) clearance on 2017-06-08. It is manufactured by Toshibamedical Systems Corporation. The 510(k) number is K171222.
When was Vitrea Software Toshiba Package; VSTP-001A approved by the FDA?
Vitrea Software Toshiba Package; VSTP-001A received FDA 510(k) clearance on 2017-06-08, under approval number K171222.
What company makes Vitrea Software Toshiba Package; VSTP-001A?
Vitrea Software Toshiba Package; VSTP-001A is manufactured by Toshibamedical Systems Corporation.
What is the FDA product code for Vitrea Software Toshiba Package; VSTP-001A?
The FDA product code for Vitrea Software Toshiba Package; VSTP-001A is LLZ.
Other Devices by Toshibamedical Systems Corporation
Related Devices (Code: LLZ)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.